Medical Monitoring jobs

A Clinical Research Coordinator (CRC) manages the daily operations of clinical trials, ensuring participant safety and protocol compliance. They recruit/screen patients, obtain informed consent, collect data, manage study documents, and report adverse events. They act as the primary liaison between investigators, sponsors, and participants.

Key Responsibilities

• Coordinate day-to-day clinical trial operations at the site
• Screen, recruit, and enroll study participants
• Obtain and document informed consent
• Schedule subject visits and follow-ups
• Collect, record, and maintain accurate study data
• Maintain regulatory documents and study files
• Ensure compliance with study protocols and GCP guidelines
• Report adverse events and safety information
• Prepare for monitoring visits, audits, and inspections
• Liaise with investigators, sponsors, and monitors

Required Qualifications

• Bachelor’s or Master’s degree in Life Sciences / Pharmacy / Nursing / Medical field

Job Types: Full-time, Permanent, Fresher

Pay: ₹18,000.00 - ₹25,000.00 per month

Benefits:

• Health insurance
• Paid sick time

Work Location: In person